449174-29-2

Upstream product

• 449174-28-1 (2S,3R,4S,5R,6R,7R)-7-(benzyloxy-diisopropyl-silanyloxy)-1-(4-methoxy-benzyloxy)-2,4,6-trimethyl-nonane-3,5-diol 
• 77-76-9 2,2-dimethoxy-propane 
• 449174-22-5 (2R,3RS)-3-(benzyloxy-diisopropyl-silanyloxy)-2-methyl-pentan-1-ol 
• 449174-21-4 (1RS,2R)-benzyloxy-[1-ethyl-3-(4-methoxy-benzyloxy)-2-methyl-propoxy]-diisopropylsilane 
• 449174-27-0 (2S,4R,5S,6R,7R)-7-(benzyloxy-diisopropyl-silanyloxy)-5-hydroxy-1-(4-methoxybenzyloxy)-2,4,6-trimethyl-nonan-3-one 
• 89238-99-3 O-(4-methoxybenzyl)-trichloroacetimidate 
• 182193-69-7 (S)-1-(p-methoxybenzyloxy)-2-methylpentan-3-one 
• 185203-71-8 methyl (S)-N-methyl-N-methoxy-3-(4-methoxybenzyloxy)-2-methylpropanoate 
• 213385-33-2 (R)-1-((4-methoxybenzyl)oxy)-2-methylpentan-3-one 
• 449173-99-3 (2R,3RS)-1-(4-methoxybenzyloxy)-2-methyl-pentan-3-ol 
• 449174-01-0 (2S,3RS)-3-(benzyloxy-diisopropyl-silanyloxy)-2-methyl-pentanal 

Relevant academic research and scientific papers

Toward the combinatorial synthesis of polyketide libraries: Asymmetric aldol reactions with α-chiral aldehydes on solid support

(Matrix presented) The viability of performing stereocontrolled aldol additions with α-chiral aldehydes attached by a silyl linker to a hydroxymethylpolystyrene resin is demonstrated for boron and titanium enolates. Subsequent ketone reduction and manipul